Refine
Language
- English (22)
Is part of the Bibliography
- yes (22)
Keywords
- Euglyphida (2)
- Soil erosion (2)
- biogenic silica (2)
- phytolith (2)
- silicon cycling (2)
- (SEM) analysis (1)
- (TPI) (1)
- Automatic chamber (1)
- Biogenic silica (1)
- Biosilicification (1)
Institute
- Institut für Umweltwissenschaften und Geographie (22) (remove)
Silicon is a beneficial element for many plants and is deposited in plant tissue as amorphous bio-opal called phytoliths. The biochemical processes of silicon uptake and precipitation induce isotope fractionation: the mass-dependent shift in the relative abundances of the stable isotopes of silicon. At the bulk scale, delta Si-30 ratios span from -2 to +6 parts per thousand. To further constrain these variations in situ, at the scale of individual phytolith fragments, we used femtosecond laser ablation multi-collector inductively coupled plasma-mass spectrometry (fsLA-MC-ICP-MS). A variety of phytoliths from grasses, trees and ferns were prepared from plant tissue or extracted from soil. Good agreement between phytolith delta Si-30 ratios obtained by bulk solution MC-ICP-MS analysis and in situ isotope ratios from fsLA-MC-ICP-MS validates the method. Bulk solution analyses result in at least twofold better precision for delta Si-30 (2s on reference materials <= 0.11 parts per thousand) over that found for the means of in situ analyses (2s typically <= 0.24 parts per thousand). We find that bushgrass, common reed and horsetail show large internal variations up to 2 parts per thousand in delta Si-30, reflecting the various pathways of silicon from soil to deposition. Femtosecond laser ablation provides a means to identify the underlying processes involved in the formation of phytoliths using silicon isotope ratios.
Phytoliths in particulate matter released by wind erosion on arable land in La Pampa, Argentina
(2022)
Silicon (Si) is considered a beneficial element in plant nutrition, but its importance on ecosystems goes far beyond that. Various forms of silicon are found in soils, of which the phytogenic pool plays a decisive role due to its good availability. This Si returns to the soil through the decomposition of plant residues, where they then participate in the further cycle as biogenic amorphous silica (bASi) or so-called phytoliths. These have a high affinity for water, so that the water holding capacity and water availability of soils can be increased even by small amounts of ASi. Agricultural land is a considerable global dust source, and dust samples from arable land have shown in cloud formation experiments a several times higher ice nucleation activity than pure mineral dust. Here, particle sizes in the particulate matter fractions (PM) are important, which can travel long distances and reach high altitudes in the atmosphere. Based on this, the research question was whether phytoliths could be detected in PM samples from wind erosion events, what are the main particle sizes of phytoliths and whether an initial quantification was possible.Measurements of PM concentrations were carried out at a wind erosion measuring field in the province La Pampa, Argentina. PM were sampled during five erosion events with Environmental Dust Monitors (EDM). After counting and classifying all particles with diameters between 0.3 and 32 mu m in the EDMs, they are collected on filters. The filters were analyzed by Scanning Electron Microscopy and Energy Dispersive X-Ray analysis (SEM-EDX) to investigate single or ensembles of particles regarding composition and possible origins.The analyses showed up to 8.3 per cent being phytoliths in the emitted dust and up to 25 per cent of organic origin. Particles of organic origin are mostly in the coarse dust fraction, whereas phytoliths are predominately transported in the finer dust fractions. Since phytoliths are both an important source of Si as a plant nutrient and are also involved in soil C fixation, their losses from arable land via dust emissions should be considered and its specific influence on atmospheric processes should be studied in detail in the future.
Wind erosion of agricultural soils affects their stock of essential elements for plants, like phosphorus (P). It is known that the composition of the eroded sediments varies with height, according to the size and density of the transported substances. Aim of this study was to analyze the concentration and enrichment ratios of P forms in sediments transported by the wind. A wind-tunnel study was performed on a sandy-and a sandy loam soil in order to measure P forms concentrations in the saltating sediments. P concentrations were also measured in the particulate matter (PM) of each soil, gained with the Easy Dust Generator. In both soils, inorganic-(Pi) and organic P (Po) were preferentially transported in PM, with enrichment ratios of 1.8 and 5.5, respectively. Nevertheless, a Pi/Po of 0.9 indicated that the accumulation of the minor Po in PM was more pronounced than Pi. This agrees with P-rich light and easily erodible organic compounds, almost exclusively accumulated in PM, and in relatively heavy and less erodible minerals, like apatites, in lower height sediments. Labile P (Pl) was preferentially transported in saltating sediments of both soils. This was attributed to the selective Bray & Kurtz I's extraction of the abundant inorganic P forms of these sediments. Total P (Pt) copied the transport trends of Pi, the major form. According to the transporting trends, Pi and Po would be re-sedimented at longer distances from the source than Pl. Outcomes become useful for modeling the influence of wind erosion on P cycling.
Content and binding forms of heavy metals, aluminium and phosphorus in bog iron ores from Poland
(2009)
Bog iron ores are widespread in Polish wetland soils used as meadows or pastures. They are suspected to contain high concentrations of heavy metals, which are precipitated together with Fe along a redox gradient. Therefore, soils with bog iron ore might be important sources for a heavy metal transfer from meadow plants into the food chain. However, this transfer depends on the different binding forms of heavy metals. The binding forms were quantified by sequential extraction analysis of heavy metals (Fe, Mn, Cr, Co, Ni, Cd, Pb) as well as Al and P on 13 representative samples of bog iron ores from central and southwestern Poland. Our results showed total contents of Cr, Co, Ni, Zn, Cd, and Pb not to exceed the natural values for sandy soils from Poland. Only the total Mn was slightly higher. The highest contents of all heavy metals have,been obtained in iron oxide fractions V (occluded in noncrystalline and poorly crystalline Fe oxides) and VI (occluded in crystalline Fe oxides). The results show a distinct relationship between the content of Fe and the quantity of Zn and Pb as well R Water soluble as well as plant available fractions were below the detection limit in most cases. From this we concluded bog iron ores not to be an actual, important source of heavy metals in the food chain. However, a remobilization of heavy metals might occur due to any reduction of iron oxides in bog iron ores, for example, by rising groundwater levels.
Separation of coarse organic particles from bulk surface soil samples by electrostatic attraction
(2009)
Different separation procedures are suggested for studying the stability and functionality of sod organic matter (OM). Density fractionation procedures using high-molarity, water-based salt solutions to separate organic particles may cause losses or transfers of C between particle and soluble OM fractions during separation, which may be a result of solution processes. The objective of this study was to separate coarse organic particles (>0.315 mm) from air- dried surface soil samples to avoid such solution processes as far as possible. Air-dried surface soil samples (<2 mm) from nine adjacent arable and forest sites were sieved into five soil particle size fractions (2-1.25, 1.25-0.8, 0.8- 0.5, 0.5-0.4, and 0.4-0.315 mm). Coarse organic particles were separated from each of these fractions using electrostatic attraction by a charged glass surface. The sum of the total dry matter content of the electrostatically separated coarse organic particles ranged from 0.05 to 140 g kg(-1). Scanning electron microscopy images and organic C (OC) analyses indicated, however, that the coarse organic particle fractions were also composed of 20 to 76% mineral particles (i.e., 200-760 g mineral kg(-1) fraction). The repeatability of the electrostatic attraction procedure falls within a range similar to that of accepted density fractionation methods using high-molarity salt solutions. Based on the similarity in repeatability, we suggest that the electrostatic attraction procedure will successfully remove coarse organic particles (>0.315 mm) from air-dried surface soil samples. Because aqueous solutions are not used, the electrostatic attraction procedure to separate coarse organic particles avoids C losses and transfers associated with solution-dependent techniques. Therefore, this method can be used as a pretreatment for subsequent density- or solubility-based soil OM fractionation procedures.
Land use and mineral characteristics affect the ability of surface as well as subsurface soils to sequester organic carbon and their contribution to mitigation of the greenhouse effect. There is less information about the effects of land use and soil properties on the amount and composition of organic matter (OM) for subsurface soils as compared with surface soils. Here we aimed to analyse the long-term (>= 100 years) impact of arable and forest land use and soil mineral characteristics on subsurface soil organic carbon (SOC) contents, as well as on amount and composition of OM sequentially separated by Na pyrophosphate solution (OM(PY)) from subsurface soil samples. Seven soils with different mineral characteristics (Albic and Haplic Luvisol, Colluvic and Haplic Regosol, Haplic and Vertic Cambisol, Haplic Stagnosol) were selected from within Germany. Soil samples were taken from subsurface horizons of forest and adjacent arable sites continuously used for > 100 years. The OM(PY) fractions were analysed for their OC content (OC(PY)) and characterized by Fourier transform infrared spectroscopy. Multiple regression analyses for the arable subsurface soils indicated significant positive relationships between the SOC contents and combined effects of the (i) exchangeable Ca (Ca(ex)) and oxalate-soluble Fe (Fe(ox)) and (ii) the Ca(ex) and Al(ox) contents. For these soils the increase in OC (OC(PY) multiplied by the relative C=O content of OM(PY)) and increasing contents of Ca(ex) indicated that OM(PY) mainly interacts with Ca2+. For the forest subsurface soils (pH < 5), the OC(PY) contents were related to the contents of Na-pyrophosphate-soluble Fe and Al. The long-term arable and forest land use seems to result in different OM(PY)-mineral interactions in subsurface soils. On the basis of this, we hypothesize that a long-term land-use change from arable to forest may lead to a shift from mainly OM(PY)-Ca2+ to mainly OM(PY)-Fe3+ and -Al3+ interactions if the pH of subsurface soils significantly decreases to < 5.
Soil landscape research is faced with wide-ranging questions of soil erosion, precision farming, and agricultural risk management. Digital Soil Morphometrics is a powerful tool to provide respective answers or recommendations but requires soil data from the pedon-to-field scale with high horizontal and vertical resolutions, including the subsoil. We present an efficient sampling and measurement method for easily obtainable soil driving cores with low-destructive preparation. Elemental contents and soil organic and mineral matter composition were measured rapidly and in large numbers using a multi-sensor approach, i.e., visible and near infrared (Vis-NIR), diffuse reflectance infrared Fourier transform (DRIFT), and X-ray fluorescence (XRF) spectroscopy. The suitability of the approach with respect to three-dimensional soil landscape models was tested using soils along a slope representing different stages of erosion and deposition in a hummocky landscape under arable land use (Calcaric Regosols, Calcic Luvisols, Luvic Stagnosols, Gleyic-Colluvic Regosols). The combination of soil core sampling, pedological description, and three spectroscopic techniques enabled rapid determination and interpretation of horizontal and vertical spatial distributions of soil organic carbon (SOC), soil organic and mineral matter composition, as well as CaCO3, Fe, and Mn contents. Depth profiles for SOC, CaCO3, and Fe contents were suitable indicators for site-specific degrees of erosion and matter transport processes at the pedon-to-field scale. Fe and Mn profiles helped identifying zones of reductive and oxic domains in subsoils (gleyzation). Further methodical developments should implement plant-availability of nutrients, characterization of Fe oxides, and calibration of the spectroscopic techniques to field-moist samples.
Provisioning a sufficient stable source of food requires sound knowledge about current and upcoming threats to agricultural production. To that end machine learning approaches were used to identify the prevailing climatic and soil hydrological drivers of spatial and temporal yield variability of four crops, comprising 40 years yield data each from 351 counties in Germany. Effects of progress in agricultural management and breeding were subtracted from the data prior the machine learning modelling by fitting smooth non-linear trends to the 95th percentiles of observed yield data. An extensive feature selection approach was followed then to identify the most relevant predictors out of a large set of candidate predictors, comprising various soil and meteorological data. Particular emphasis was placed on studying the uniqueness of identified key predictors. Random Forest and Support Vector Machine models yielded similar although not identical results, capturing between 50% and 70% of the spatial and temporal variance of silage maize, winter barley, winter rapeseed and winter wheat yield. Equally good performance could be achieved with different sets of predictors. Thus identification of the most reliable models could not be based on the outcome of the model study only but required expert's judgement. Relationships between drivers and response often exhibited optimum curves, especially for summer air temperature and precipitation. In contrast, soil moisture clearly proved less relevant compared to meteorological drivers. In view of the expected climate change both excess precipitation and the excess heat effect deserve more attention in breeding as well as in crop modelling.
Due to the fact that silicon (Si) increases the resistance of plants against diverse abiotic and biotic stresses, Si nowadays is categorized as beneficial substance for plants. However, humans directly influence Si cycling on a global scale. Intensified agriculture and corresponding harvest-related Si exports lead to Si losses in agricultural soils. This anthropogenic desilication might be a big challenge for modern agriculture. However, there is still only little knowledge about Si cycling in agricultural systems of the temperate zone, because most studies focus on rice and sugarcane production in (sub)tropical areas. Furthermore, many studies are performed for a short term only, and thus do not provide the opportunity to analyze slow changes in soil-plant systems (e.g., desilication) over long periods. We analyzed soil and plant samples from an ongoing long-term field experiment (established 1963) in the temperate zone (NE Germany) to evaluate the effects of different nitrogen-phosphoruspotassium (NPK) fertilization rates and crop straw recycling (i.e., straw incorporation) on anthropogenic desilication in the long term. Our results clearly show that crop straw recycling not only prevents anthropogenic desilication (about 43-60% of Si exports can be saved by crop straw recycling in the long term), but also replenishes plant available Si stocks of agricultural soil-plant systems. Furthermore, we found that a reduction of N fertilization rates of about 69% is possible without considerable biomass losses. This economy of the need for N fertilizers potentially can be combined with the benefits of crop straw recycling, i.e., enhancement of carbon sequestration via straw inputs and prevention of anthropogenic desilication of agricultural soil-plant systems. Thus crop straw recycling might have the potential to act as key management practice in sustainable, low fertilization agriculture in the temperate zone in the future.
The detection of auto-fluorescence in phytogenic, hydrated amorphous silica depositions (phytoliths) has been found to be a promising approach to verify if phytoliths were burnt or not, especially in archaeological contexts. However, it is unknown so far at what temperature and how auto-fluorescence is induced in phytoliths. We used fluorescence microscopy, scanning electron microscope-energy dispersive X-ray spectroscopy (SEM-EDX), and Fourier transform infrared spectroscopy to analyze auto-fluorescence in modern phytoliths extracted from plant samples or in intact leaves of winter wheat. Leaves and extracted phytoliths were heated at different temperatures up to 600 degrees C. The aims of our experiments were i) to find out what temperature is needed to induce auto-fluorescence in phytoliths, ii) to detect temperature-dependent changes in the molecular structure of phytoliths related to auto-fluorescence, and iii) to derive a mechanistic understanding of auto-fluorescence in phytoliths. We found organic compounds associated with phytoliths to cause auto-fluorescence in phytoliths treated at temperatures below approx. 400 degrees C. In phytoliths treated at higher temperatures, i.e., 450 and 600 degrees C, phytolith auto-fluorescence was mainly caused by molecular changes of phytolith silica. Based on our results we propose that auto-fluorescence in phytoliths is caused by clusterization-triggered emissions, which are caused by overlapping electron clouds forming non-conventional chromophores. In phytoliths heated at temperatures above about 400 degrees C dihydroxylation and the formation of siloxanes result in oxygen clusters that serve as non-conventional chromophores in fluorescence events. Furthermore, SEM-EDX analyses revealed that extractable phytoliths were dominated by lumen phytoliths (62%) compared to cell wall phytoliths (38%). Our findings might be not only relevant in archaeological phytolith-based examinations, but also for studies on the temperature-dependent release of silicon from phytoliths and the potential of long-term carbon sequestration in phytoliths.